Emma Clement
Impact in
- Genetics top 5%
- Neurogenetic and Muscular Disorders Research
- Genomics and Rare Diseases
- Immunology and Allergy top 5%
- Cell Adhesion Molecules Research
Papers in
-
- Muscle Physiology and Disorders 11
- Ubiquitin and proteasome pathways 3
- Ion channel regulation and function 2
- Genetics 9
- Genomics and Rare Diseases 7
- Neurogenetic and Muscular Disorders Research 3
- Co-authors
- Caroline Godfrey (5 shared papers)A. Reghan Foley (1 shared paper)Francesco Muntoni (1 shared paper)Eugenio Mercuri (7 shared papers)Francesco Muntoni (6 shared papers)Caroline A. Sewry (7 shared papers)Stephen Abbs (6 shared papers)C. Jimenez‐Mallebrera (5 shared papers)
- Journals
- Neuromuscular Disorders (5 papers)Neuroradiology (3 papers)American Journal of Neuroradiology (3 papers)Annals of Neurology (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
Emma Clement
34 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 77
- Genetics 178
- Immunology and Allergy 93
- Molecular Biology 899
- Cardiology and Cardiovascular Medicine 195
- Genetics 251
Countries citing papers authored by Emma Clement
This map shows the geographic impact of Emma Clement's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Emma Clement with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emma Clement more than expected).
Fields of papers citing papers by Emma Clement
This network shows the impact of papers produced by Emma Clement. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Emma Clement. The network helps show where Emma Clement may publish in the future.
Co-authors
The 25 scholars most cited alongside Emma Clement, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 172 | |
| 2 | 2010 | 138 | |
| 3 | 2006 | 108 | |
| 4 | 2009 | 107 | |
| 5 | 2009 | 105 | |
| 6 | 2018 | 89 | |
| 7 | 2008 | 89 | |
| 8 | 2011 | 66 | |
| 9 | 2008 | 57 | |
| 10 | 2020 | 41 | |
| 11 | 2012 | 41 | |
| 12 | 2019 | 41 | |
| 13 | Muscular dystrophies due to defective glycosylation of dystroglycan. | 2007 | 37 |
| 14 | 2016 | 36 | |
| 15 | 2016 | 33 | |
| 16 | 2020 | 19 | |
| 17 | 2017 | 15 | |
| 18 | 2009 | 14 | |
| 19 | 2019 | 13 | |
| 20 | 2020 | 13 |
About Emma Clement
Emma Clement is a scholar working on Molecular Biology, Genetics, Genetics, Sensory Systems and Surgery, having authored 40 papers that have together received 1.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (11 papers), Genomics and Rare Diseases (7 papers), Hearing, Cochlea, Tinnitus, Genetics (4 papers), Ubiquitin and proteasome pathways (3 papers), Neurogenetic and Muscular Disorders Research (3 papers), Calcium signaling and nucleotide metabolism (2 papers), Cellular transport and secretion (2 papers) and Ion channel regulation and function (2 papers). The work is most often cited by research in Genetics (178 citations), Immunology and Allergy (93 citations), Molecular Biology (899 citations), Cardiology and Cardiovascular Medicine (195 citations) and Genetics (251 citations). Emma Clement has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Caroline Godfrey, A. Reghan Foley, Francesco Muntoni, Eugenio Mercuri, Francesco Muntoni, Caroline A. Sewry, Stephen Abbs, C. Jimenez‐Mallebrera, R. Mein and Lucy Feng. Their work appears in journals such as Neuromuscular Disorders, Neuroradiology, American Journal of Neuroradiology, Annals of Neurology and Journal of Medical Genetics.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.